U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C10H9I3O3
Molecular Weight 557.8901
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PHENOBUTIODIL

SMILES

CCC(OC1=C(I)C=C(I)C=C1I)C(O)=O

InChI

InChIKey=VYAGDYWTCWDKIS-UHFFFAOYSA-N
InChI=1S/C10H9I3O3/c1-2-8(10(14)15)16-9-6(12)3-5(11)4-7(9)13/h3-4,8H,2H2,1H3,(H,14,15)

HIDE SMILES / InChI
Phenobutiodil was used as the contrast medium in radiology. As a diagnostic aid in cholecystography. Conjugated phenobutiodil (Biliodyl) in the small and large bowel can be recognized by its fine, homogeneous appearance.

Approval Year

PubMed

PubMed

TitleDatePubMed
[Recent triiodinated contrast media for oral cholecystocholangiography].
1985-02
The significance of conjugated phenobutiodil (biliodyl) in the intestine in the absence of gallbladder opacification a preliminary assessment.
1977-05
[Clinical studies with the oral billary contrast medium baygnostil].
1959-12-05
[Experiences with the triiodated oral gallbladder contrast medium baygnostil].
1959-01-30
[Baygnostil, a new triiodized oral biliary contrast medium].
1958-12
[Use of the oral contrast medium baygnostil in cholecystography].
1958-11-08
[Oral cholecystography with baygnostil].
1957-12-13
[Baygnostil, a new contrast medium in cholecystography, & its practical trial].
1957-11-02
A comparative trial of telepaque and biliodyl in 50 cases.
1957-07

Sample Use Guides

In Vivo Use Guide
Single dose of 3 g (six tablets)
Route of Administration: Oral
Name Type Language
PHENOBUTIODIL [MI]
Preferred Name English
PHENOBUTIODIL
INN   MI   WHO-DD  
INN  
Official Name English
Phenobutiodil [WHO-DD]
Common Name English
2-(2,4,6-TRIIODOPHENOXY)BUTYRIC ACID
Systematic Name English
phenobutiodil [INN]
Common Name English
Code System Code Type Description
INN
473
Created by admin on Mon Mar 31 19:29:08 GMT 2025 , Edited by admin on Mon Mar 31 19:29:08 GMT 2025
PRIMARY
EVMPD
SUB09772MIG
Created by admin on Mon Mar 31 19:29:08 GMT 2025 , Edited by admin on Mon Mar 31 19:29:08 GMT 2025
PRIMARY
ChEMBL
CHEMBL2104664
Created by admin on Mon Mar 31 19:29:08 GMT 2025 , Edited by admin on Mon Mar 31 19:29:08 GMT 2025
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DRUG CENTRAL
3812
Created by admin on Mon Mar 31 19:29:08 GMT 2025 , Edited by admin on Mon Mar 31 19:29:08 GMT 2025
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CAS
554-24-5
Created by admin on Mon Mar 31 19:29:08 GMT 2025 , Edited by admin on Mon Mar 31 19:29:08 GMT 2025
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MERCK INDEX
m883
Created by admin on Mon Mar 31 19:29:08 GMT 2025 , Edited by admin on Mon Mar 31 19:29:08 GMT 2025
PRIMARY Merck Index
SMS_ID
100000082238
Created by admin on Mon Mar 31 19:29:08 GMT 2025 , Edited by admin on Mon Mar 31 19:29:08 GMT 2025
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NCI_THESAURUS
C166909
Created by admin on Mon Mar 31 19:29:08 GMT 2025 , Edited by admin on Mon Mar 31 19:29:08 GMT 2025
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FDA UNII
67F5J7GUUR
Created by admin on Mon Mar 31 19:29:08 GMT 2025 , Edited by admin on Mon Mar 31 19:29:08 GMT 2025
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MESH
C008831
Created by admin on Mon Mar 31 19:29:08 GMT 2025 , Edited by admin on Mon Mar 31 19:29:08 GMT 2025
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EPA CompTox
DTXSID80862188
Created by admin on Mon Mar 31 19:29:08 GMT 2025 , Edited by admin on Mon Mar 31 19:29:08 GMT 2025
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PUBCHEM
11127
Created by admin on Mon Mar 31 19:29:08 GMT 2025 , Edited by admin on Mon Mar 31 19:29:08 GMT 2025
PRIMARY
ECHA (EC/EINECS)
209-065-1
Created by admin on Mon Mar 31 19:29:08 GMT 2025 , Edited by admin on Mon Mar 31 19:29:08 GMT 2025
PRIMARY